SURGICAL FACE MASK-EAR LOOP
K-Number: K891051 · 1989-04-12
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Device Summary
Frequently Asked Questions
What is the SURGICAL FACE MASK-EAR LOOP?
SURGICAL FACE MASK-EAR LOOP is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is Dispomed, Inc.. The 510(k) number is K891051.
When did SURGICAL FACE MASK-EAR LOOP receive FDA 510(k) clearance?
SURGICAL FACE MASK-EAR LOOP received FDA 510(k) clearance on 1989-04-12, under 510(k) number K891051.
Who is the listed applicant for SURGICAL FACE MASK-EAR LOOP?
The FDA 510(k) record lists Dispomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGICAL FACE MASK-EAR LOOP?
The FDA product code for SURGICAL FACE MASK-EAR LOOP is FXX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Dispomed, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FXX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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